TY - JOUR
T1 - BEAM Conditioning Regimen Has Higher Toxicity Compared With High-Dose Melphalan for Salvage Autologous Hematopoietic Stem Cell Transplantation in Multiple Myeloma
AU - Veeraputhiran, Muthu
AU - Jain, Tania
AU - Deol, Abhinav
AU - Ayash, Lois
AU - Kim, Seongho
AU - Dyson, Gregory
AU - Bhutani, Divaya
AU - Lum, Lawrence G.
AU - Ratanatharathorn, Voravit
AU - Uberti, Joseph P.
AU - Abidi, Muneer H.
PY - 2015/9/1
Y1 - 2015/9/1
N2 - Background Salvage autologous stem cell transplantation (ASCT) is increasingly used for eligible patients with multiple myeloma (MM) for progress after conventional chemotherapy. We recently used BEAM (BCNU, etoposide, cytarabine, and melphalan) conditioning for patients with myeloma receiving salvage ASCT whose disease progressed after a first ASCT with high-dose melphalan (HDM). We report safety and efficacy of BEAM salvage ASCT in MM in comparison with HDM-based salvage ASCT. Patients and Methods Between 2008 and 2013, 43 consecutive patients received salvage ASCT for MM (19 with HDM; 24 with BEAM). Results The BEAM group had a higher incidence of infections, intensive level of care, and fever (19 vs. 13 patients; P =.02), whereas the melphalan group had a higher incidence of mucositis (7 vs. 2 patients; P =.03). Other toxicities were not different. There was no significant difference in disease status and response rate before and after salvage ASCT between the 2 groups. The median time of follow-up after salvage ASCT was 5 and 9 months and the median progression-free survival (PFS) times were 7.7 and 12.1 months (P =.82) for BEAM and melphalan, respectively. Conclusion BEAM seemed to be associated with higher toxicity with comparable efficacy to HDM ASCT. Longer follow-up is needed to determine whether there is any significant difference in PFS between the 2 groups.
AB - Background Salvage autologous stem cell transplantation (ASCT) is increasingly used for eligible patients with multiple myeloma (MM) for progress after conventional chemotherapy. We recently used BEAM (BCNU, etoposide, cytarabine, and melphalan) conditioning for patients with myeloma receiving salvage ASCT whose disease progressed after a first ASCT with high-dose melphalan (HDM). We report safety and efficacy of BEAM salvage ASCT in MM in comparison with HDM-based salvage ASCT. Patients and Methods Between 2008 and 2013, 43 consecutive patients received salvage ASCT for MM (19 with HDM; 24 with BEAM). Results The BEAM group had a higher incidence of infections, intensive level of care, and fever (19 vs. 13 patients; P =.02), whereas the melphalan group had a higher incidence of mucositis (7 vs. 2 patients; P =.03). Other toxicities were not different. There was no significant difference in disease status and response rate before and after salvage ASCT between the 2 groups. The median time of follow-up after salvage ASCT was 5 and 9 months and the median progression-free survival (PFS) times were 7.7 and 12.1 months (P =.82) for BEAM and melphalan, respectively. Conclusion BEAM seemed to be associated with higher toxicity with comparable efficacy to HDM ASCT. Longer follow-up is needed to determine whether there is any significant difference in PFS between the 2 groups.
KW - Autologous stem cell transplantation
KW - BEAM
KW - Conditioning therapy
KW - Engraftment
KW - Salvage therapy
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U2 - 10.1016/j.clml.2015.05.008
DO - 10.1016/j.clml.2015.05.008
M3 - Article
C2 - 26166312
AN - SCOPUS:84939571216
SN - 2152-2650
VL - 15
SP - 531
EP - 535
JO - Clinical Lymphoma, Myeloma and Leukemia
JF - Clinical Lymphoma, Myeloma and Leukemia
IS - 9
M1 - 611
ER -